List of variants in gene combination LOC126860794, NOTCH1 reported as uncertain significance by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_017617.5(NOTCH1):c.5971C>T (p.Arg1991Cys)	rs759553984	0.00001
NM_017617.5(NOTCH1):c.6061G>A (p.Val2021Ile)	rs759643831	0.00001
NM_017617.5(NOTCH1):c.6010C>T (p.Arg2004Cys)	rs1589054589

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